HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetramethyl orthocarbonate → 4-benzyloxy-2-methoxy-1-methyl-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetramethyl orthocarbonate | HCID 74613 | — |
| Reactant | 2-amino-3-benzyloxy-N-methylaniline | HCID 10489541 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-benzyloxy-2-methoxy-1-methyl-1H-benzimidazole | HCID 10754361 | — |
Reaction Steps
To a stirred solution of 2-amino-3-benzyloxy-N-methylaniline (318.5 mg) in acetic acid (3.2 ml) was added tetramethyl orthocarbonate (223.0 μl) at ambient temperature, and the reaction mixture was stirred for 4 hours. The reaction mixture was concentrated in vacuo, and to the residue were added ethyl acetate and a saturated sodium bicarbonate solution. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was triturated with n-hexane-diisopropyl ether to give 4-benzyloxy-2-methoxy-1-methyl-1H-benzimidazole (273.3 mg) as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06008229 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-d7d1ba524b8c4248ad6b1cfa84899827 |
| Source note | uspto-grants-1999_12 |